Osmorespiratory Compromise in Zebrafish (Danio rerio): Effects of Hypoxia and Acute Thermal Stress on Oxygen Consumption, Diffusive Water Flux, and Sodium Net Loss Rates.

IF 1.4 4区 生物学 Q4 DEVELOPMENTAL BIOLOGY
Zebrafish Pub Date : 2020-12-01 DOI:10.1089/zeb.2020.1947
John O Onukwufor, Chris M Wood
{"title":"Osmorespiratory Compromise in Zebrafish (<i>Danio rerio</i>): Effects of Hypoxia and Acute Thermal Stress on Oxygen Consumption, Diffusive Water Flux, and Sodium Net Loss Rates.","authors":"John O Onukwufor,&nbsp;Chris M Wood","doi":"10.1089/zeb.2020.1947","DOIUrl":null,"url":null,"abstract":"<p><p>The traditional thesis of the osmorespiratory compromise is that low branchial water and ion permeability would be traded off for increased O<sub>2</sub> permeability at times of elevated O<sub>2</sub> demand. However, there is growing evidence of independent regulation of these permeabilities in hypoxia-tolerant fish. Using 0.5-g zebrafish previously maintained under normoxia at 25°C, we investigated responses to acute temperature challenges (15°C or 35°C), acute hypoxia (15 min at 10% or 5% air saturation), as well as longer-term exposures to 10% hypoxia, on O<sub>2</sub> consumption (MO<sub>2</sub>), diffusive water flux, and net sodium loss rates. Exposure to 35°C increased, and 15°C decreased all three rates, with diffusive water flux showing the lowest temperature sensitivity, and Na<sup>+</sup> loss the greatest. Acute 10% and 5% hypoxia increased diffusive water flux and net Na<sup>+</sup> loss, and it reduced MO<sub>2</sub>. All these responses reflected the traditional osmorespiratory compromise. However, during prolonged 10% hypoxia, MO<sub>2</sub> recovered, diffusive water flux decreased below control levels, and Na<sup>+</sup> loss rate remained elevated, even during posthypoxia recovery. Overall, zebrafish do not fit standard patterns previously seen in either hypoxia-tolerant or -intolerant fish but are clearly able to adjust the effective permeabilities of their gills to O<sub>2</sub>, water, and ions independently during acute temperature and hypoxia exposures.</p>","PeriodicalId":23872,"journal":{"name":"Zebrafish","volume":"17 6","pages":"400-411"},"PeriodicalIF":1.4000,"publicationDate":"2020-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/zeb.2020.1947","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zebrafish","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1089/zeb.2020.1947","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
引用次数: 6

Abstract

The traditional thesis of the osmorespiratory compromise is that low branchial water and ion permeability would be traded off for increased O2 permeability at times of elevated O2 demand. However, there is growing evidence of independent regulation of these permeabilities in hypoxia-tolerant fish. Using 0.5-g zebrafish previously maintained under normoxia at 25°C, we investigated responses to acute temperature challenges (15°C or 35°C), acute hypoxia (15 min at 10% or 5% air saturation), as well as longer-term exposures to 10% hypoxia, on O2 consumption (MO2), diffusive water flux, and net sodium loss rates. Exposure to 35°C increased, and 15°C decreased all three rates, with diffusive water flux showing the lowest temperature sensitivity, and Na+ loss the greatest. Acute 10% and 5% hypoxia increased diffusive water flux and net Na+ loss, and it reduced MO2. All these responses reflected the traditional osmorespiratory compromise. However, during prolonged 10% hypoxia, MO2 recovered, diffusive water flux decreased below control levels, and Na+ loss rate remained elevated, even during posthypoxia recovery. Overall, zebrafish do not fit standard patterns previously seen in either hypoxia-tolerant or -intolerant fish but are clearly able to adjust the effective permeabilities of their gills to O2, water, and ions independently during acute temperature and hypoxia exposures.

斑马鱼的渗透呼吸损害:缺氧和急性热应激对氧气消耗、扩散水通量和钠净损失率的影响。
传统的渗透呼吸妥协理论认为,当氧气需求增加时,低的鳃水和离子渗透性会被交换为增加的氧气渗透性。然而,越来越多的证据表明,在耐缺氧的鱼类中,这些渗透性是独立调节的。我们将0.5 g的斑马鱼置于25°C的常氧环境中,研究了它们在急性温度(15°C或35°C)、急性缺氧(10%或5%空气饱和度15分钟)以及长期暴露于10%缺氧环境下对氧气消耗(MO2)、扩散水通量和净钠损失率的反应。暴露于35°C时,这三种速率均升高,15°C时,这三种速率均降低,扩散水通量表现出最低的温度敏感性,Na+损失最大。10%和5%的急性缺氧增加了扩散水通量和净Na+损失,降低了MO2。这些反应都反映了传统的渗透呼吸妥协。然而,在长时间的10%缺氧期间,MO2恢复,弥漫性水通量低于对照水平,Na+损失率仍然升高,即使在缺氧后恢复期间也是如此。总的来说,斑马鱼不符合先前在耐缺氧或不耐缺氧鱼类中看到的标准模式,但显然能够在急性温度和缺氧暴露中独立调节其鳃对O2,水和离子的有效渗透性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Zebrafish
Zebrafish DEVELOPMENTAL BIOLOGY-ZOOLOGY
CiteScore
3.60
自引率
5.00%
发文量
29
审稿时长
3 months
期刊介绍: Zebrafish is the only peer-reviewed journal dedicated to the central role of zebrafish and other aquarium species as models for the study of vertebrate development, evolution, toxicology, and human disease. Due to its prolific reproduction and the external development of the transparent embryo, the zebrafish is a prime model for genetic and developmental studies. While genetically more distant from humans, the vertebrate zebrafish nevertheless has comparable organs and tissues, such as heart, kidney, pancreas, bones, and cartilage. Zebrafish introduced the new section TechnoFish, which highlights these innovations for the general zebrafish community. TechnoFish features two types of articles: TechnoFish Previews: Important, generally useful technical advances or valuable transgenic lines TechnoFish Methods: Brief descriptions of new methods, reagents, or transgenic lines that will be of widespread use in the zebrafish community Zebrafish coverage includes: Comparative genomics and evolution Molecular/cellular mechanisms of cell growth Genetic analysis of embryogenesis and disease Toxicological and infectious disease models Models for neurological disorders and aging New methods, tools, and experimental approaches Zebrafish also includes research with other aquarium species such as medaka, Fugu, and Xiphophorus.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信